A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689026



Internal ID15078992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92865431..92868641hg38UCSC Ensembl
Innerchr6:93575149..93578359hg19UCSC Ensembl
Innerchr6:93631870..93635080hg18UCSC Ensembl
Innerchr6:93631870..93635080hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383211
hg193211
hg183211
hg173211
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689026
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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